Inova Health System - Falls Church, VA

posted 3 months ago

Full-time - Entry Level
Falls Church, VA
Hospitals

About the position

The Clinical Research Coordinator I at Inova Health System plays a crucial role in implementing research studies while ensuring the protection of research subjects and compliance with regulatory standards. This position involves overseeing the entire research process from site selection to study closure, ensuring that all aspects of the study are conducted ethically and efficiently. The coordinator will be responsible for coordinating the financial elements of study implementation, managing everything from protocol feasibility to the final stages of the study. This role requires a basic understanding of study coordination and the ability to perform various tasks under direct supervision, making it an excellent opportunity for those looking to grow in the field of clinical research. The Clinical Research Coordinator I will participate in a variety of clinical studies, which may include investigational products, different study phases, and various therapeutic areas and indications. This position is designed for individuals who are eager to learn and develop their skills in clinical research, as they will be guided by experienced professionals in the field. The coordinator will also be expected to explain key protocol elements, ensure subject safety, and adhere to Good Clinical Practice (GCP) guidelines throughout the study process. This role is essential in maintaining the integrity of clinical research at Inova and ensuring that all studies are conducted in compliance with ethical standards and regulatory requirements.

Responsibilities

  • Identifies and explains key protocol elements and performs study tasks under direct supervision.
  • Explains basic elements of subject safety including the reasoning behind the required use of an Institutional Review Board/Independent Ethics Committee, study activity documentation, and event reporting requirements.
  • Demonstrates subject protection under direct supervision.
  • Explains the investigational products development process and identifies key regulations to control these processes.
  • Explains and performs study operational activities in compliance with Good Clinical Practice (GCP), and non-GCP related study management activities.
  • Explains how to document data according to ALCOA-C (Attributable, Legible, Contemporaneous, Original, Accurate and Complete) principles.
  • Other duties as assigned.

Requirements

  • Associate degree or relevant experience in lieu of degree.
  • Two years of patient care experience or one year of clinical research experience with a bachelor's degree.

Benefits

  • Health, Vision, and Dental Coverage
  • Life Insurance
  • Short/Long Term Disability
  • 4 weeks Paid Parental Leave
  • Retirement plan with dollar-for-dollar match up to 5%
  • Competitive salary based on experience
  • Paid Time Off accrued from the first day of work
  • Educational Assistance of up to $5,250/year
  • Student Loan Refinancing
  • Adoption Assistance
  • Child Care Centers
  • Scholarship Program
  • Free Parking
  • Exclusive savings opportunities to in-store events, theme parks, discounts, movie tickets, and local offerings.
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